Jens Schallner

1.2k total citations
15 papers, 324 citations indexed

About

Jens Schallner is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Jens Schallner has authored 15 papers receiving a total of 324 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Genetics. Recurrent topics in Jens Schallner's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (3 papers). Jens Schallner is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (3 papers). Jens Schallner collaborates with scholars based in Germany, Austria and United Kingdom. Jens Schallner's co-authors include Andreas Rump, Luisa Mackenroth, Maja von der Hagen, Bernd Wollnik, Jörg Striessnig, Filippo Beleggia, Alexandra Pinggera, Evelin Schröck, Nataliya Di Donato and Karl Hackmann and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and The Journal of Pediatrics.

In The Last Decade

Jens Schallner

15 papers receiving 324 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jens Schallner Germany 11 182 120 55 50 43 15 324
Mefford Hc 6 163 0.9× 90 0.8× 21 0.4× 35 0.7× 28 0.7× 239 337
Louise Benarroch France 9 159 0.9× 102 0.8× 41 0.7× 46 0.9× 17 0.4× 17 296
Sandra Whalen France 13 268 1.5× 157 1.3× 41 0.7× 59 1.2× 33 0.8× 28 417
Devon Lamb Thrush United States 10 218 1.2× 141 1.2× 25 0.5× 54 1.1× 13 0.3× 19 334
Marcello Scala Italy 15 207 1.1× 178 1.5× 32 0.6× 53 1.1× 22 0.5× 61 513
Valeria Cinquina Italy 11 112 0.6× 193 1.6× 15 0.3× 40 0.8× 44 1.0× 22 388
Sonya A. Gunter United States 4 237 1.3× 166 1.4× 29 0.5× 54 1.1× 22 0.5× 4 400
Ziad Rifai United States 8 232 1.3× 50 0.4× 62 1.1× 66 1.3× 27 0.6× 9 361
Göran Brandberg Sweden 8 244 1.3× 116 1.0× 96 1.7× 35 0.7× 80 1.9× 10 442
Pasqua Cancellara Italy 10 283 1.6× 49 0.4× 24 0.4× 41 0.8× 33 0.8× 10 430

Countries citing papers authored by Jens Schallner

Since Specialization
Citations

This map shows the geographic impact of Jens Schallner's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jens Schallner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jens Schallner more than expected).

Fields of papers citing papers by Jens Schallner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jens Schallner. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jens Schallner. The network helps show where Jens Schallner may publish in the future.

Co-authorship network of co-authors of Jens Schallner

This figure shows the co-authorship network connecting the top 25 collaborators of Jens Schallner. A scholar is included among the top collaborators of Jens Schallner based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jens Schallner. Jens Schallner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

15 of 15 papers shown
1.
Weiss, Deike, Anna Perez, P. Weber, et al.. (2024). Cognitive function in SMA patients with 2 or 3 SMN2 copies treated with SMN-modifying or gene addition therapy during the first year of life. European Journal of Paediatric Neurology. 51. 17–23. 12 indexed citations
2.
Kleefeld, Felix, Andreas Hentschel, Arpad von Moers, et al.. (2023). Beyond vacuolar pathology: Multiomic profiling of Danon disease reveals dysfunctional mitochondrial homeostasis. Neuropathology and Applied Neurobiology. 49(4). e12920–e12920. 3 indexed citations
3.
Pirozzi, Filomena, Nicole Horsley, William B. Dobyns, et al.. (2021). Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes. American Journal of Medical Genetics Part A. 185(9). 2719–2738. 16 indexed citations
4.
Smitka, Martin, Jens Schallner, Katja Akgün, et al.. (2021). Serum neurofilament light chain in pediatric spinal muscular atrophy patients and healthy children. Annals of Clinical and Translational Neurology. 8(10). 2013–2024. 44 indexed citations
5.
Becker, Lena‐Luise, Hormos Salimi Dafsari, Jens Schallner, et al.. (2020). The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification. Journal of Human Genetics. 65(11). 1003–1017. 31 indexed citations
6.
Alter, Svenja, Alrun Hotz, Arne Jahn, et al.. (2018). Novel VPS33B mutation in a patient with autosomal recessive keratoderma‐ichthyosis‐deafness syndrome. American Journal of Medical Genetics Part A. 176(12). 2862–2866. 8 indexed citations
7.
Gieldon, Laura, Luisa Mackenroth, Anne‐Karin Kahlert, et al.. (2018). Diagnostic value of partial exome sequencing in developmental disorders. PLoS ONE. 13(8). e0201041–e0201041. 29 indexed citations
8.
Porrmann, Joseph, Nataliya Di Donato, Anne‐Karin Kahlert, et al.. (2017). Novel PRPS1 gain‐of‐function mutation in a patient with congenital hyperuricemia and facial anomalies. American Journal of Medical Genetics Part A. 173(10). 2736–2742. 11 indexed citations
9.
Gieldon, Laura, Luisa Mackenroth, Andreas Rump, et al.. (2017). Skewed X‐inactivation in a family with DLG3‐associated X‐linked intellectual disability. American Journal of Medical Genetics Part A. 173(9). 2545–2550. 12 indexed citations
10.
Pinggera, Alexandra, Luisa Mackenroth, Andreas Rump, et al.. (2017). New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsy. Human Molecular Genetics. 26(15). 2923–2932. 74 indexed citations
11.
Westenberger, Ana, Norbert Brüggemann, Aloysius Domingo, et al.. (2016). Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases. The Journal of Pediatrics. 181. 306–308.e1. 25 indexed citations
12.
13.
Mackenroth, Luisa, Karl Hackmann, Jens Schallner, et al.. (2015). 6q22.33 microdeletion in a family with intellectual disability, variable major anomalies, and behavioral abnormalities. American Journal of Medical Genetics Part A. 167(11). 2800–2807. 2 indexed citations
14.
Hackmann, Karl, Jens Schallner, Evelin Schröck, et al.. (2013). Severe intellectual disability, West syndrome, Dandy–Walker malformation, and syndactyly in a patient with partial tetrasomy 17q25.3. American Journal of Medical Genetics Part A. 161(12). 3144–3149. 13 indexed citations
15.
Endris, Volker, Karl Hackmann, Teresa Neuhann, et al.. (2010). Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia. American Journal of Medical Genetics Part A. 152A(11). 2908–2911. 43 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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